Canonical Allele Identifier: CA2338594528
Gene: SIX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766891C= , CM000681.2:g.45766891C= GRCh38
NC_000019.9:g.46270149C= , CM000681.1:g.46270149C= GRCh37
NC_000019.8:g.50961989C= NCBI36
NG_012745.1:g.7349G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1068G= MANE Select ENSP00000316842.4:p.Leu356=
ENST00000317578.6:c.1068G= ENSP00000316842.4:p.Leu356=
ENST00000560160.1:c.587-780G=
ENST00000560168.1:c.*256G= ENSP00000453189.2:n.*256G=
ENST00000622857.1:c.16-929G= ENSP00000481365.1:n.16-929G=
NM_175875.4:c.1068G= NP_787071.2:p.Leu356=
NM_175875.5:c.1068G= MANE Select NP_787071.3:p.Leu356=